Evidence map›Paper›PMID 32678222›Full record

ArticleScientific reports2020

The mechanisms of ameliorating effect of a green tea polyphenol on diabetic nephropathy based on diacylglycerol kinase α.

Daiki Hayashi, Liuqing Wang, Shuji Ueda, Minoru Yamanoue, Hitoshi Ashida, Yasuhito Shirai

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  12. PP2 Ameliorates Renal Fibrosis by Regulating the NF-Oxidative medicine and cellular longevity · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Daiki HayashiDepartment of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Kobe University, Rokkodai-Cho 1-1, Nada-Ku, Kobe, 657-8501, Japan.
Liuqing WangDepartment of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Kobe University, Rokkodai-Cho 1-1, Nada-Ku, Kobe, 657-8501, Japan.
Shuji UedaDepartment of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Kobe University, Rokkodai-Cho 1-1, Nada-Ku, Kobe, 657-8501, Japan.
Minoru YamanoueDepartment of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Kobe University, Rokkodai-Cho 1-1, Nada-Ku, Kobe, 657-8501, Japan.
Hitoshi AshidaDepartment of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Kobe University, Rokkodai-Cho 1-1, Nada-Ku, Kobe, 657-8501, Japan.
Yasuhito ShiraiDepartment of Applied Chemistry in Bioscience, Graduate School of Agricultural Science, Kobe University, Rokkodai-Cho 1-1, Nada-Ku, Kobe, 657-8501, Japan. shirai@kobe-u.ac.jp.
Kobe University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Significant efforts have been made to ameliorate diabetic nephropathy (DN) by inhibiting protein kinase C. However, these efforts have not been successful in human trials, suggesting that novel therapeutic strategies are required. Thus far, it has been reported that green tea polyphenol epigallocatechin gallate (EGCg) improved albuminuria in DN in a human trial. Our previous study revealed that activation of diacylglycerol kinase α (DGKα) plays a crucial role in the amelioration of DN and that EGCg activates DGKα. Here, we investigated whether and how DGKα contributes to the amelioration of DN upon stimulation by EGCg by using streptozotocin-induced type 1 diabetic model mice. Our results revealed that EGCg ameliorated albuminuria in DN through DGKα in vivo, and methylated EGCg, which has higher absorption in the plasma improved albuminuria in DN effectively. Additionally, we showed that c-Src mediated EGCg-induced DGKα translocation and colocalized with the 67 kDa laminin receptor, which is an EGCg receptor. Furthermore, EGCg attenuated the loss of podocytes in DN by preventing a decrease in focal adhesion under high glucose conditions. Our results indicate that the DGKα pathway is an attractive therapeutic target and that activating this pathway is a novel strategy for treating DN.

Indexed as

AnimalsBiomarkersDiabetic NephropathiesDiacylglycerol KinaseDisease Models, AnimalFluorescent Antibody TechniqueHumansImmunohistochemistryMaleMiceModels, BiologicalPlant ExtractsPodocytesPolyphenolsTeaBiomarkersDiacylglycerol KinasePlant ExtractsPolyphenolsTea

Identifiers

PMID32678222
PMCPMC7366667
OpenAlexW3043001684

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.